Matches in Nanopublications for { ?s ?p "[Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_assertion description "[Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.
- NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_assertion description "[Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_provenance.